WO2003059807A2 - Crystalline solids of carvedilol and processes for their preparation - Google Patents
Crystalline solids of carvedilol and processes for their preparation Download PDFInfo
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- WO2003059807A2 WO2003059807A2 PCT/US2003/001137 US0301137W WO03059807A2 WO 2003059807 A2 WO2003059807 A2 WO 2003059807A2 US 0301137 W US0301137 W US 0301137W WO 03059807 A2 WO03059807 A2 WO 03059807A2
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- carvedilol
- crystalline
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- solvate
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
Definitions
- This invention relates to a novel crystalline solid of carvedilol or a solvate thereof, to processes for its preparation, to compositions containing it and to its use in medicine. This invention further relates to a novel process for preparing crystalline carvedilol Form II.
- Carvedilol ( ⁇ )- 1 -(Carbazol-4-yloxy)-3 - [ [2-(o-methoxyphenoxy) ethyl] amino] -2- propanol, is a nonselective ⁇ -adrenergic blocker with ( ⁇ -blocking activity.
- Carvedilol is a racemic mixture having the following structural formula:
- Carvedilol is the active ingredient of CORECr ® , which is indicated for the treatment of congestive heart failure and for the management of hypertension. Since carvedilol is a multiple-action drug, its beta-blocking activity affects the response to certain nerve impulses in parts of the body. As a result, beta-blockers decrease the heart's need for blood and oxygen by reducing its workload. Carvedilol is also known to be a vasodilator resulting primarily from alpha-adrenoceptor blockade. The multiple actions of carvedilol are responsible for the antihypertensive efficacy of the drug and for its effectiveness in managing congestive heart failure.
- Form I was generated by dissolving crude carvedilol in methanol, heating the solution, cooling the solution, and stirring the solution for a time sufficient to produce Form I.
- Form II was generated by recrystallizing Form I in 2-propanol.
- the present invention relates to the solid state physical properties of carvedilol. These properties can be influenced by controlling the conditions under which carvedilol is obtained in solid form.
- Solid state physical properties include, for example, the flowability of the milled solid. Flowability affects the ease with which the material is handled during processing into a pharmaceutical product. When particles of the powdered compound do not flow past each other easily, a formulation specialist must take that fact into account in developing a tablet or capsule formulation, which may necessitate the use of glidants such as colloidal silicon dioxide, talc, starch or tribasic calcium phosphate.
- Another important solid state property of a pharmaceutical compound is its rate of dissolution in aqueous fluid.
- the rate of dissolution of an active ingredient in a patient's stomach fluid can have therapeutic consequences since it imposes an upper limit on the rate at which an orally-administered active ingredient can reach the patient's bloodstream.
- the rate of dissolution is also a consideration in formulating syrups, elixirs and other liquid medicaments.
- the solid state form of a compound may also affect its behavior on compaction and its storage stability.
- polymorphic form may give rise to tliermal behavior different from that of the amorphous material or another polymorphic form.
- Thermal behavior is measured in the laboratory by such techniques as capillary melting point, thermogravimetric analysis (TGA) and differential scanning calorimetric (DSC) and can be used to distinguish some polymorphic forms from others.
- TGA thermogravimetric analysis
- DSC differential scanning calorimetric
- a particular polymorphic form may also give rise to distinct spectroscopic properties that may be detectable by powder X-ray crystallography, solid state 13 C NMR spectrometry and infrared spectrometry.
- the present invention also relates to solvates of carvedilol.
- a substance crystallizes out of solution, it may trap molecules of solvent at regular intervals in the crystal lattice. Solvation also affects utilitarian physical properties of the solid state like flowability and dissolution rate.
- a pharmaceutical compound which can form polymorphs or solvates, is its solubility in aqueous solution, particularly the solubility in gastric juices of a patient.
- Other important properties relate to the ease of processing the form into pharmaceutical dosages, such as the tendency of a powdered or granulated form to flow and the surface properties that determine whether crystals of the form will adhere to each other when compacted into a tablet.
- the present invention provides a crystalline solid of carvedilol or a solvate thereof characterized by data selected from the group consisting of a PXRD pattern with peaks at about 6.5, 7.3, 16.0, and 30.5 ⁇ 0.2 degrees two-theta, a PXRD pattern with peaks at about 5.8, 10.7, 11.1, 11.5, 13.1, 13.7, 16.8, 17.7, 18.5, and 23.0 ⁇ 0.2 degrees two-theta, a DSC thermogram with endothermic peaks at about 74° C and 112° C, and a FTIR spectrum with peaks at about 613, 740, 994, 1125, 1228, 1257, 1441, 1508, 1737, 2840, 3281, 3389, and 3470 cm “1 .
- Said solid crystalline form denotes Form VI.
- the present invention provides a process for preparing a crystalline solid of carvedilol or a solvate thereof having at least one characteristic of Form VI (such as the PXRD peaks and/or FTIR peaks, and/or DSC peaks disclosed herein).
- carvedilol is contacted with ethyl acetate to form a solution.
- the solution is cooled and optionally seeded with carvedilol Form II.
- the solution can be stirred under high velocity agitation to form a suspension, which then can be cooled under high velocity agitation.
- the present invention provides a process for preparing a crystalline solid of carvedilol Form II, including the steps of heating crystalline carvedilol having at least one characteristic of Form VI until the crystalline carvedilol is dry, mixing carvedilol Form II with the dry crystalline carvedilol, and storing the mixture for a holding time sufficient to transform the dry crystalline carvedilol into Form II.
- Figure 1 is a PXRD pattern for carvedilol Form VI.
- Figure 2 is a FTIR spectrum for carvedilol Form VI.
- Figure 3 is a DSC thermogram for carvedilol Form VI.
- Figure 4 is a DTG thermogram for carvedilol Form VI.
- the present invention provides a novel crystalline solid of carvedilol or a solvate thereof, designated Form VI.
- Carvedilol solvate Form VI is characterized by a PXRD pattern (Fig. 1) with peaks at about 6.5, 7.3, 16.0, and 30.5 ⁇ 0.2 degrees two-theta. Further PXRD peaks were observed at about 5.8, 10.7, 11.1, 11.5, 13.1, 13.7, 16.8, 17.7, 18.5, and 23.0 ⁇ 0.2 degrees two-theta.
- Carvedilol solvate Form VI produces a FTIR spectrum (Fig. 2) with characteristic absorption bands at about 613, 740, 994, 1125, 1228, 1257, 1441, 1508, 1737, 2840, 3281, 3389, and 3470 cm " 4 Further FTIR peaks were observed at about 720, 1100, 1286, 1454, 1589, 2911, and 2935 cm " 4
- Carvedilol solvate Form VI produces a Differential Thermal Gravimetry (DTG) thermogram (Fig. 4) showing a weight loss step in the temperature range of 35-104° C of about 13%. This value is equal to the expected value corresponding to two molecules of ethyl acetate per three molecules of carvedilol.
- the water content of carvedilol solvate Form VI was tested by Karl-Fisher titration, which showed it to be free of water.
- the present invention provides a novel process for preparing a crystalline solid of carvedilol or a solvate thereof, involving the steps of contacting carvedilol with ethyl acetate to form a solution, cooling the solution optionally under agitation.
- the starting carvedilol is dry.
- the solution can optionally be seeded with carvedilol Form II.
- the solution can be stirred under high velocity agitation to form a suspension, which then can be cooled under high velocity agitation.
- the product obtained by this process has at least one characteristic of Form VI, and can be separated from the ethyl acetate by conventional means such as filtration.
- the product can also be dried.
- the mixture of ethyl acetate and dry carvedilol is heated to a temperature in the range of about 65° to about 80° C, most preferably in the range of about 70° to about 77° C to form a solution. Thereafter, preferably, the temperature of the solution is reduced to between about 40° to about 55° C, most preferably between about 46° to about 50° C.
- the seeded solution is stirred at a temperature in the range of about 46° C to about 50° C for a holding time sufficient to precipitate Form VI.
- a holding time of about 30 minutes under high velocity agitation (at least 260 rpm) is typically sufficient.
- the temperature of the suspension is preferably cooled to about 10° C for a holding time, preferably about 3 hours under high velocity agitation.
- the cooled suspension should be stirred for about 30 minutes.
- the present invention provides a process for preparing a crystalline solid of carvedilol Form II, including the steps of heating crystalline carvedilol having at least one characteristic of Form VI until the crystalline carvedilol is dry, mixing carvedilol Form II with the dry crystalline carvedilol, and storing the mixture for a holding time sufficient to transform the dry crystalline carvedilol into Form II.
- crystalline carvedilol having at least one characteristic of Form VI is heated to a temperate in the range of about 50° to about 60° C, and most preferably to about 55° C.
- the heating step can be preformed at atmospheric pressure or under reduced pressure.
- the pressure is about 60 mm Hg, and more preferably about 30 mm Hg.
- Crystalline carvedilol having at least one characteristic of Form VI is typically dry after about 16 hours of heating.
- Dry crystalline carvedilol having at least one characteristic of Form VI is mixed with carvedilol Form II and stored for a holding time sufficient to transform the dry crystalline carvedilol into Form II. A holding time of from about 1 week to about 2 weeks is typically sufficient.
- Carvedilol Form I can also be present.
- Carvedilol Form VI can be milled into a powder and used in a pharmaceutical product or physically modified such as by granulation to produce larger granules of carvedilol Form VI.
- Carvedilol Form VI can also be used to prepare a liquid pharmaceutical product by dissolving or dispersing it in a liquid medium such as water, glycerin, vegetable oil and the like as discussed in greater detail below.
- Carvedilol Form VI is useful for treating patients with congestive heart failure and hypertension and for producing a hypotensive effect in mammals, including human patients.
- Carvedilol Form VI can be formulated into a variety of compositions for administration to humans and mammals.
- compositions of the present invention contain carvedilol Form VI, optionally in mixture with other crystalline forms and/or other active ingredients such as hydrochlorothiazide.
- the pharmaceutical compositions of the present invention can contain one or more excipients. Excipients are added to the composition for a variety of purposes. Diluents increase the bulk of a solid pharmaceutical composition and can make a pharmaceutical dosage form containing the composition easier for the patient and caregiver to handle. Diluents for solid compositions include, for example, microcrystalline cellulose (e.g.
- Binders for solid pharmaceutical compositions include acacia, alginic acid, carbomer (e.g. carbopol), carboxymethylcellulose sodium, dextrin, ethyl cellulose, gelatin, guar gum, hydrogenated vegetable oil, hydroxyethyl cellulose, hydroxypropyl cellulose (e.g. Klucel ® ), hydroxypropyl methyl cellulose (e.g. Methocel ® ), liquid glucose, magnesium aluminum silicate, maltodextrin, methylcellulose, polymethacrylates, povidone (e.g. Kollidon ® , Plasdone ® ), pregelatinized starch, sodium alginate and starch.
- carbomer e.g. carbopol
- carboxymethylcellulose sodium dextrin
- ethyl cellulose gelatin
- guar gum hydrogenated vegetable oil
- hydroxyethyl cellulose hydroxypropyl cellulose
- hydroxypropyl methyl cellulose e.g.
- the dissolution rate of a compacted solid pharmaceutical composition in the patient's stomach can be increased by the addition of a disintegrant to the composition.
- Disintegrants include alginic acid, carboxymethylcellulose calcium, carboxymethylcellulose sodium (e.g. Ac-Di-Sol ® , Primellose ® ), colloidal silicon dioxide, croscarmellose sodium, crospovidone (e.g. Kollidon , Polyplasdone ® ), guar gum, magnesium aluminum silicate, methyl cellulose, microcrystalline cellulose, polacrilin potassium, powdered cellulose, pregelatinized starch, sodium alginate, sodium starch glycolate (e.g. Explotab ® ) and starch.
- alginic acid include alginic acid, carboxymethylcellulose calcium, carboxymethylcellulose sodium (e.g. Ac-Di-Sol ® , Primellose ® ), colloidal silicon dioxide, croscarmellose sodium, crospovidone (e.g
- Glidants can be added to improve the flow properties of non-compacted solid composition and improve the accuracy of dosing.
- Excipients that can function as glidants include colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, starch, talc and tribasic calcium phosphate.
- a dosage form such as a tablet is made by compaction of a powdered composition
- the composition is subjected to pressure from a punch and dye.
- Some excipients and active ingredients have a tendency to adhere to the surfaces of the punch and dye, which can cause the product to have pitting and other surface irregularities.
- a lubricant can be added to the composition to reduce adhesion and ease release of the product form the dye.
- Lubricants include magnesium stearate, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated castor oil, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc and zinc stearate.
- Flavoring agents and flavor enhancers make the dosage form more palatable to the patient.
- Common flavoring agents and flavor enhancers for pharmaceutical products that can be included in the composition of the present invention include maltol, vanillin, ethyl vanillin, menthol, citric acid, fumaric acid, ethyl maltol, and tartaric acid.
- Solid and liquid compositions can also be dyed using any pharmaceutically acceptable colorant to improve their appearance and/or facilitate patient identification of the product and unit dosage level.
- liquid pharmaceutical compositions of the present invention carvedilol Form VI and any other solid excipients are dissolved or suspended in a liquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene glycol or glycerin.
- a liquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene glycol or glycerin.
- Liquid pharmaceutical compositions can contain emulsifying agents to disperse uniformly throughout the composition an active ingredient or other excipient that is not soluble in the liquid carrier.
- Emulsifying agents that can be useful in liquid compositions of the present invention include, for example, gelatin, egg yolk, casein, cholesterol, acacia, tragacanth, chondrus, pectin, methyl cellulose, carbomer, cetostearyl alcohol and cetyl alcohol.
- Liquid pharmaceutical compositions of the present invention can also contain a viscosity-enhancing agent to improve the mouth-feel of the product and or coat the lining of the gastrointestinal tract.
- a viscosity-enhancing agent include acacia, alginic acid bentonite, carbomer, carboxymethylcellulose calcium or sodium, cetostearyl alcohol, methyl cellulose, ethylcellulose, gelatin guar gum, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, maltodextrin, polyvinyl alcohol, povidone, propylene carbonate, propylene glycol alginate, sodium alginate, sodium starch glycolate, starch tragacanth and xanthan gum.
- Sweetening agents such as sorbitol, saccharin, sodium saccharin, sucrose, aspartame, fructose, mannitol and invert sugar can be added to improve the taste.
- Preservatives and chelating agents such as alcohol, sodium benzoate, butylated hydroxy toluene, butylated hydroxyanisole and ethylenediamine tetraacetic acid can be added at levels safe for ingestion to improve storage stability.
- a liquid composition according to the present invention can also contain a buffer such as guconic acid, lactic acid, citric acid or acetic acid, sodium guconate, sodium lactate, sodium citrate or sodium acetate. Selection of excipients and the amounts to use can be readily determined by the formulation scientist based upon experience and consideration of standard procedures and reference works in the field.
- a buffer such as guconic acid, lactic acid, citric acid or acetic acid, sodium guconate, sodium lactate, sodium citrate or sodium acetate.
- the solid compositions of the present invention include powders, granulates, aggregates and compacted compositions.
- Carvedilol Form VI can be administered for treatment of congestive heart failure and hypertension by any means that delivers the active ingredient(s) to the site of the body where beta-blocking activity exerts a therapeutic effect on the patient.
- administration can be oral, buccal, parenteral (including subcutaneous, intramuscular, and intravenous) rectal, inhalant and ophthalmic.
- the most suitable route in any given case will depend on the nature and severity of the condition being treated, the most preferred route of the present invention is oral.
- Carvedilol Form VI can be conveniently administered to a patient in oral unit dosage form and prepared by any of the methods well-known in the pharmaceutical arts. Dosage forms include solid dosage forms like tablets, powders, capsules, sachets, troches and lozenges as well as liquid syrups, suspensions and elixirs.
- compositions and dosage forms can be prepared by wet granulation. In wet granulation some or all of the active ingredients and excipients in powder form are blended and then further mixed in the presence of a liquid, typically water, that causes the powders to clump up into granules. The granulate is screened and/or milled, dried and then screened and/or milled to the desired particle size. The granulate can then be tableted or other excipients can be added prior to tableting such as a glidant and or lubricant.
- a liquid typically water
- a tableting composition can be prepared conventionally by dry blending.
- the blended composition of the actives and excipients can be compacted into a slug or a sheet and then comminuted into compacted granules.
- the compacted granules can be compressed subsequently into a tablet.
- a blended composition can be compressed directly into a compacted dosage form using direct compression techniques.
- Direct compression produces a more uniform tablet without granules.
- Excipients that are particularly well suited to direct compression tableting include microcrystalline cellulose, spray dried lactose, dicalcium phosphate dihydrate and colloidal silica. The proper use of these and other excipients in direct compression tableting is known to those in the art with experience and skill in particular formulation challenges of direct compression tableting.
- a capsule filling of the present invention can comprise any of the aforementioned blends and granulates that were described with reference to tableting, only they are not subjected to a final tableting step.
- a tablet can, for example, be formulated by blending and directly compressing the composition in a tablet machine.
- a capsule can, for example, be prepared by filling half of a gelatin capsule with the above tablet composition and capping it with the other half of the gelatin capsule.
- a simple parenteral solution for injection can, for example, be prepared by combining carvedilol Form VI, sterile propylene glycol, and sterile water and sealing the composition in a sterile vial under sterile conditions.
- Capsules, tablets and lozenges and other unit dosage forms preferably contain a dosage level of about 1 mg to about 100 mg of carvedilol Form VI.
- the following examples are given for the purpose of illustrating the present invention and shall not be construed as limiting the scope or spirit of the invention.
- thermogravimetric curves were obtained by methods known in the art using a Mettler Toledo DSC821 6 .
- the weight of the samples was about 3-5 mg.
- the temperature range was from about 30° C to at least 250° C, at the rate of 10° C/minute.
- thermogravimetric curves were also obtained by methods known in the art using a Shimadzu DTG-50.
- the temperature range was from about 30° C to at least 250° C, at the rate of 10° C/minute. Samples were purged with nitrogen gas at a flow rate of 20 ml/min.
- the FTIR spectra were obtained by methods known in the art, such as diffuse reflectance, using a Perkin-Elmer, Spectrum One FTIR Spectrometer.
- the scanning parameters were as follows: range: 4000-400 cm “1 , 16 scans, resolution: 4.0 cm "1 .
- Example 1 Carvedilol Form VI Dry carvedilol (7 Kg) was added to ethyl acetate (70 L) and heated to about 70-77° C under agitation. After complete dissolution, the solution was cooled to about 46-50° C under agitation. The solution was then seeded with carvedilol Form II and stirred at a temperature of about 46-50° C for about 30 minutes under high velocity agitation (at least 260 rpm). The resulting suspension was cooled to a temperature of about 10° C over a period of 3 hours under high velocity agitation. The suspension was stirred for an addition 30 minutes and then filtered to obtain carvedilol Form VI.
- Example 2 Carvedilol Form II Three trays containing carvedilol Form VI ( 1 Kg per tray) were inserted into a vacuum oven, heated to about 55° C under vacuum of 30 mm Hg and dried for about 16 hours. Immediately after drying, the polymorphic content of the dried sample was a mixture of Form VI and Form II. After storage at room temperature for about 4 weeks, a mixture of Form I, Form II and Form VI were found.
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Abstract
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Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03703815A EP1474133A4 (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation |
MXPA04006909A MXPA04006909A (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation. |
AU2003205146A AU2003205146A1 (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation |
JP2003559922A JP2005515226A (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and methods for preparing them |
KR10-2004-7010875A KR20040077872A (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation |
CA002472377A CA2472377A1 (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation |
IS7351A IS7351A (en) | 2002-01-15 | 2004-07-13 | Solid crystalline carvedilol and methods for producing them |
HR20040673A HRP20040673A2 (en) | 2002-01-15 | 2004-07-21 | Crystalline solids of carvedilol and processes for their preparation |
NO20043383A NO20043383L (en) | 2002-01-15 | 2004-08-13 | Solid crystalline substances of carvedilol and processes for their preparation |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US34931002P | 2002-01-15 | 2002-01-15 | |
US60/349,310 | 2002-01-15 |
Publications (2)
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WO2003059807A2 true WO2003059807A2 (en) | 2003-07-24 |
WO2003059807A3 WO2003059807A3 (en) | 2003-12-04 |
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Application Number | Title | Priority Date | Filing Date |
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PCT/US2003/001137 WO2003059807A2 (en) | 2002-01-15 | 2003-01-15 | Crystalline solids of carvedilol and processes for their preparation |
Country Status (14)
Country | Link |
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US (3) | US6710184B2 (en) |
EP (1) | EP1474133A4 (en) |
JP (1) | JP2005515226A (en) |
KR (1) | KR20040077872A (en) |
CN (1) | CN1298322C (en) |
AU (1) | AU2003205146A1 (en) |
CA (1) | CA2472377A1 (en) |
HR (1) | HRP20040673A2 (en) |
IS (1) | IS7351A (en) |
MX (1) | MXPA04006909A (en) |
NO (1) | NO20043383L (en) |
PL (1) | PL371409A1 (en) |
WO (1) | WO2003059807A2 (en) |
ZA (1) | ZA200405443B (en) |
Cited By (8)
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WO2005021504A2 (en) * | 2003-09-02 | 2005-03-10 | Krka, Tovarna Zdravil, D.D., Novo Mesto | New crystalline forms of carvedilol |
WO2006135757A1 (en) * | 2005-06-09 | 2006-12-21 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of carvedilol and processes for their preparation |
WO2007043938A1 (en) * | 2005-10-07 | 2007-04-19 | Astrazeneca Ab | NOVEL CRYSTALLINE FORM OF 3,5-DIBROMO-N- [ (2S) -2- (-4- FLUOROPHENYL) -4- (3-MORPHOLIN-4-YLAZTIDIN-l-YL) BUTYL] -N METHYLBENZAMIDE, MODIFICATION B |
WO2008122105A1 (en) * | 2007-04-04 | 2008-10-16 | Apotex Inc. | Novel amorphous form of carvedilol phosphate and processes for the preparation thereof |
US7485663B2 (en) | 2000-06-28 | 2009-02-03 | Teva Pharmaceutical Industries Ltd. | Carvedilol |
US7514467B2 (en) | 2002-01-15 | 2009-04-07 | Teva Pharmaceutical Industries Ltd. | Crystalline solids of carvedilol and processes for their preparation |
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CA2483054A1 (en) * | 2002-04-30 | 2003-11-13 | Sb Pharmco Puerto Rico Inc. | Carvedilol monocitrate monohydrate |
US20050261355A1 (en) * | 2002-06-27 | 2005-11-24 | Sb Pharmco Puerto Rico Inc., | Carvedilol hydobromide |
EP1534270A4 (en) * | 2002-06-27 | 2006-05-17 | Sb Pharmco Inc | Carvedilol phosphate salts and/or solvates thereof, correspondinq compositions, and/or methods of treatment |
US20040152756A1 (en) * | 2002-07-15 | 2004-08-05 | Wei Chen | Carvedilol polymorph |
US7468442B2 (en) * | 2003-04-21 | 2008-12-23 | Matrix Laboratories Ltd. | Process for the preparation of carvedilol form-II |
US20050037040A1 (en) * | 2003-08-13 | 2005-02-17 | Moshe Arkin | Topical compositions of urea and ammonium lactate |
US20050036953A1 (en) * | 2003-08-13 | 2005-02-17 | Moshe Arkin | Topical compositions of ammonium lactate |
US20050042182A1 (en) * | 2003-08-13 | 2005-02-24 | Moshe Arkin | Topical compositions of urea |
US20050042268A1 (en) * | 2003-07-16 | 2005-02-24 | Chaim Aschkenasy | Pharmaceutical composition and method for transdermal drug delivery |
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Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
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US7605274B2 (en) | 2000-06-28 | 2009-10-20 | Teva Pharmaceutical Industries Ltd | Carvedilol |
US7485663B2 (en) | 2000-06-28 | 2009-02-03 | Teva Pharmaceutical Industries Ltd. | Carvedilol |
US7598396B2 (en) | 2002-01-15 | 2009-10-06 | Teva Pharmaceutical Industries Ltd | Crystalline solids of carvedilol and processes for their preparation |
US7514467B2 (en) | 2002-01-15 | 2009-04-07 | Teva Pharmaceutical Industries Ltd. | Crystalline solids of carvedilol and processes for their preparation |
WO2005021504A3 (en) * | 2003-09-02 | 2005-06-02 | Krka Tovarna Zdravil D D Novo | New crystalline forms of carvedilol |
WO2005021504A2 (en) * | 2003-09-02 | 2005-03-10 | Krka, Tovarna Zdravil, D.D., Novo Mesto | New crystalline forms of carvedilol |
WO2006135757A1 (en) * | 2005-06-09 | 2006-12-21 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of carvedilol and processes for their preparation |
WO2007043938A1 (en) * | 2005-10-07 | 2007-04-19 | Astrazeneca Ab | NOVEL CRYSTALLINE FORM OF 3,5-DIBROMO-N- [ (2S) -2- (-4- FLUOROPHENYL) -4- (3-MORPHOLIN-4-YLAZTIDIN-l-YL) BUTYL] -N METHYLBENZAMIDE, MODIFICATION B |
US8022094B2 (en) | 2006-06-28 | 2011-09-20 | Teva Pharmaceutical Industries Ltd. | Carvedilol phosphate |
US8114900B2 (en) | 2006-06-28 | 2012-02-14 | Teva Pharmaceutical Industries Ltd. | Amorphous carvedilol dihydrogen phosphate |
US8124644B2 (en) | 2006-06-28 | 2012-02-28 | Teva Pharmaceutical Industries Ltd. | Carvedilol phosphate |
WO2008122105A1 (en) * | 2007-04-04 | 2008-10-16 | Apotex Inc. | Novel amorphous form of carvedilol phosphate and processes for the preparation thereof |
US11065237B2 (en) | 2013-11-15 | 2021-07-20 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid, compositions, and uses thereof |
US11690836B2 (en) | 2013-11-15 | 2023-07-04 | Akebia Therapeutics, Inc. | Solid forms of {[5-(3-chlorophenyl)-3-hydroxypyridine-2-carbonyl]amino}acetic acid, compositions, and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
US20030166702A1 (en) | 2003-09-04 |
JP2005515226A (en) | 2005-05-26 |
US6710184B2 (en) | 2004-03-23 |
HRP20040673A2 (en) | 2005-06-30 |
AU2003205146A1 (en) | 2003-07-30 |
ZA200405443B (en) | 2005-07-08 |
CN1298322C (en) | 2007-02-07 |
NO20043383L (en) | 2004-08-13 |
US7514467B2 (en) | 2009-04-07 |
CN1615133A (en) | 2005-05-11 |
CA2472377A1 (en) | 2003-07-24 |
KR20040077872A (en) | 2004-09-07 |
US20090163721A1 (en) | 2009-06-25 |
EP1474133A4 (en) | 2006-02-01 |
US7598396B2 (en) | 2009-10-06 |
IS7351A (en) | 2004-07-13 |
US20040171665A1 (en) | 2004-09-02 |
PL371409A1 (en) | 2005-06-13 |
WO2003059807A3 (en) | 2003-12-04 |
MXPA04006909A (en) | 2005-04-19 |
EP1474133A2 (en) | 2004-11-10 |
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